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肺炎球菌特异性CD4 T细胞反应减弱与老年时调节性T细胞增加有关。

Diminished Pneumococcal-Specific CD4 T-Cell Response is Associated With Increased Regulatory T Cells at Older Age.

作者信息

He Samantha W J, van de Garde Martijn D B, Pieren Daan K J, Poelen Martien C M, Voß Franziska, Abdullah Mohammed R, Hammerschmidt Sven, van Els Cécile A C M

机构信息

Centre for Infectious Disease Control, National Institute for Public Health and the Environment, Bilthoven, Netherlands.

Department of Molecular Genetics and Infection Biology, Interfaculty Institute of Genetics and Functional Genomics, Center for Functional Genomics of Microbes, University of Greifswald, Greifswald, Germany.

出版信息

Front Aging. 2021 Nov 3;2:746295. doi: 10.3389/fragi.2021.746295. eCollection 2021.

Abstract

Respiratory infection caused by is a leading cause of morbidity and mortality in older adults. Acquired CD4 T cell mechanism are essential for the protection against colonization and subsequent development of infections by . In this study, we hypothesized that age-related changes within the CD4 T-cell population compromise CD4 T-cell specific responses to , thereby contributing to increased susceptibility at older age. To this end, we interrogated the CD4 T-cell response against the immunogenic pneumococcal protein AliB, part of the unique oligopeptide ABC transporter system responsible for the uptake of nutrients for the bacterium and crucial for the development of pneumococcal meningitis, in healthy young and older adults. Specifically, proliferation of CD4 T cells as well as concomitant cytokine profiles and phenotypic markers implied in immunosenescence were studied. Older adults showed decreased AliB-induced CD4 T-cell proliferation that is associated with an increased frequency of regulatory T cells and lower levels of active CD25CD127CTLA-4TIGITCD4T cells. Additionally, levels of pro-inflammatory cytokines IFNy and IL-17F were decreased at older age. Our findings indicate that key features of a pneumococcal-specific CD4 T-cell immune response are altered at older age, which may contribute to enhanced susceptibility for pneumococcal infections.

摘要

由[病原体名称未给出]引起的呼吸道感染是老年人发病和死亡的主要原因。获得性CD4 T细胞机制对于预防[病原体名称未给出]的定植及随后感染的发展至关重要。在本研究中,我们假设CD4 T细胞群体中与年龄相关的变化会损害CD4 T细胞对[病原体名称未给出]的特异性反应,从而导致老年人易感性增加。为此,我们在健康的年轻人和老年人中研究了针对免疫原性肺炎球菌蛋白AliB的CD4 T细胞反应,AliB是独特的寡肽ABC转运系统的一部分,负责为细菌摄取营养,对肺炎球菌脑膜炎的发展至关重要。具体而言,研究了CD4 T细胞的增殖以及免疫衰老中涉及的伴随细胞因子谱和表型标志物。老年人显示AliB诱导的CD4 T细胞增殖减少,这与调节性T细胞频率增加以及活性CD25CD127CTLA-4TIGITCD4T细胞水平降低有关。此外,促炎细胞因子IFNy和IL-17F的水平在老年时降低。我们的研究结果表明,肺炎球菌特异性CD4 T细胞免疫反应的关键特征在老年时发生改变,这可能导致对肺炎球菌感染的易感性增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffef/9261371/9434fc799924/fragi-02-746295-g001.jpg

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